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Human GNB2 Knockdown Cell Line (Wb-Validated) #C63512

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RT-qPCR analysis. HeLa cells were infected with GNB2-specific shRNA lentiviral particles, total RNA was extracted from wild-type and knockdown cells, RT-qPCR was performed using gene-specific primers. ∆Ct (CtKD-CtWT) was used to calculate mRNA reduction (%) between wild-type and knockdown cells using the following formula: (1-1/2∆Ct) x 100%.
Western blotting analysis. GNB2 protein expression in wild-type (WT) and shRNA knockdown (KD) HeLa cells was detected using Western blotting. β-Tubulin served as a loading control. The blots were incubated with primary antibodies against GNB2 and β-Tubulin, respectively, followed by incubating with HRP-conjugated goat anti-rabbit secondary antibody. Images were developed using FeQ™ ECL Substrate Kit.
  • 基因名:
    GNB2
  • 货号:
    C63512
  • 应用:
  • 物种反应性:
规格:
1 Kit
价格:
询价
Information
Product Name Human GNB2 Knockdown Cell Line (Wb-Validated)
Aliases GNB2; Transducin Beta Chain 2; Signal-Transducing Guanine Nucleotide-Binding Regulatory Protein Beta Subunit 2; Guanine Nucleotide Binding Protein (G Protein), Beta Polypeptide 2; Guanine Nucleotide-Binding Protein G(I)/G(S)/G(T) Beta Subunit 2; Guanine Nucleotide-Binding Protein G(I)/G(S)/G(T) Subunit Beta-2; G Protein, Beta-2 Subunit; G Protein Subunit Beta-2; Heterotrimeric Guanine Nucleotide-Binding Protein 2C1; Epididymis Secretory Sperm Binding Protein; SSS4; NEDHYDF; HG2C1;SSS4
Background

Gene Name: GNB2

NCBI Gene Entry: 2783

Storage Store at liquid nitrogen for 1 year.
Kit Components 1. Human GNB2 Knockdown Cell Line (Wb-Validated)
2. Wild-type cell line
Parental Cell Line Human cell line supplied by the client
Validation Methods RT-qPCR, Western blotting (WB)
Shipping Shipped on Dry Ice.
Instructions For Use This knockdown cell line should be paired with wild-type cell line for use.
Note This product is for research use only.
Picture
  • RT-qPCR analysis. HeLa cells were infected with GNB2-specific shRNA lentiviral particles, total RNA was extracted from wild-type and knockdown cells, RT-qPCR was performed using gene-specific primers. ∆Ct (CtKD-CtWT) was used to calculate mRNA reduction (%) between wild-type and knockdown cells using the following formula: (1-1/2∆Ct) x 100%.
  • Western blotting analysis. GNB2 protein expression in wild-type (WT) and shRNA knockdown (KD) HeLa cells was detected using Western blotting. β-Tubulin served as a loading control. The blots were incubated with primary antibodies against GNB2 and β-Tubulin, respectively, followed by incubating with HRP-conjugated goat anti-rabbit secondary antibody. Images were developed using FeQ™ ECL Substrate Kit.
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RT-qPCR analysis. HeLa cells were infected with GNB2-specific shRNA lentiviral particles, total RNA was extracted from wild-type and knockdown cells, RT-qPCR was performed using gene-specific primers. ∆Ct (CtKD-CtWT) was used to calculate mRNA reduction (%) between wild-type and knockdown cells using the following formula: (1-1/2∆Ct) x 100%.
Western blotting analysis. GNB2 protein expression in wild-type (WT) and shRNA knockdown (KD) HeLa cells was detected using Western blotting. β-Tubulin served as a loading control. The blots were incubated with primary antibodies against GNB2 and β-Tubulin, respectively, followed by incubating with HRP-conjugated goat anti-rabbit secondary antibody. Images were developed using FeQ™ ECL Substrate Kit.
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